Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1016023706
Device Listing 1016023706
Listing Summary
#
Listing key
1016023706
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15607
9613183
1000227792
ORFIT INDUSTRIES NV
1
N
2026-01-01
9A, VOSVELD WIJNEGEM Antwerpen BE B-2110